Junior Quality Assurance (QA) Contractor

Discover International; España; A distancia; EUR 30.000 - 40.000; A tiempo parcial

Descripción de la vacante

A leading biotech recruitment firm is seeking a Junior Quality Assurance Contractor in Spain. This role focuses on documentation management and compliance support within a fast-paced biotech environment. Ideal candidates will have at least 2 years of experience in Quality Assurance and familiarity with pharmaceutical regulations. Strong organisational skills and digital QA tool proficiency are a plus.

Formación

• Minimum of 2 years experience in a Quality Assurance role.
• Familiarity with pharmaceutical regulations and guidelines.
• Strong written and verbal communication skills.

Responsabilidades

• Maintain and manage quality documentation systems and metrics.
• Monitor and support the QA helpdesk.
• Oversee accurate record keeping and documentation practices.
• Collaborate with global QA teams for consistency.

Conocimientos

Organisational skills

Communication skills

Detail-oriented

Time management

Familiarity with QA digital tools

Educación

Experience in Quality Assurance or regulated documentation

Herramientas

Document control systems

Quality management systems

Descripción del empleo

Junior Quality Assurance Contractor

Location: Europe | Experience Level: Junior

Overview

We are recruiting for a Junior QA Contractor with circa 2-5 years of experience, to support our client's Quality Assurance function. This role has a strong focus on documentation management and compliance related support activities. This is an excellent opportunity for someone looking to develop their QA career within a dynamic and fast paced biotech environment.

Key Responsibilities

• Maintain and manage quality documentation systems, trackers, and dashboards/metrics.
• Monitor and support the QA helpdesk, ensuring timely and accurate responses.
• Oversee accurate record keeping and documentation practices.
• May support audit coordination activities.
• Collaborate with global QA teams to ensure consistency and alignment of quality processes.
• Assist in the implementation and upkeep of quality systems and digital tools.

Qualifications & Requirements

• Minimum of 2 years experience in a Quality Assurance or regulated documentation role (within the biotechnology, pharmaceutical or life sciences sector).
• Familiarity with pharmaceutical regulations and guidelines (e.g., GMP, GCP, GVP, GLP, GDP).
• Excellent organisational and time management skills, must be able to juggle priorities.
• Strong written and verbal communication skills; able to work collaboratively across teams.
• Proactive, detail oriented mindset with a willingness to learn and take initiative.
• Ideally will be comfortable using digital QA tools and systems (e.g., document control systems, trackers, dashboards).

Seniority level

• Associate

Employment type

• Contract

Job function

• Quality Assurance, Administrative, and Science

Industries

• Pharmaceutical Manufacturing
• Biotechnology Research
• Manufacturing